Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46892
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dc.contributor.authorSondu, S-
dc.contributor.authorSethuram, B-
dc.contributor.authorRao, T Navaneeth-
dc.date.accessioned2019-03-28T05:47:02Z-
dc.date.available2019-03-28T05:47:02Z-
dc.date.issued1989-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46892-
dc.description1096-1099en_US
dc.description.abstractTransition metal ions like Ag(I), Mn(II), Cu(II), Co(II), Ni(II) have been employed as homogeneous catalysts in Ce(IV)-diacetone alcohol (DAA) redox reaction. The order in [Ce(IV)] is unity and that in [catalyst] or [substrate] fractional. The rate laws observed with all these metal ions have been found to be the same, suggesting the mechanism of catalysis to be similar. A mechanism, involving formation of a complex between the catalyst and DAA in a fast step followed. by oxidation of this complex by Ce(IV) in the slow step to the higher oxidation state complex before collapsing to give the products, is proposed. A linear correlation has been obtained between log k" (bimolecular rate constant) and K (formation constant of the complex) for the electron transfer step between metal ion catalyst and DAA.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.28A(12) [December 1989]en_US
dc.titleLinear free energy relationships in Ce(IV)-diacetone alcohol redox system catalysed by metal ionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(12) [December 1989]

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